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胃腺癌中CDKN1A组蛋白乙酰化与基因表达的关系

CDKN1A histone acetylation and gene expression relationship in gastric adenocarcinomas.

作者信息

Wisnieski Fernanda, Calcagno Danielle Queiroz, Leal Mariana Ferreira, Santos Leonardo Caires, Gigek Carolina Oliveira, Chen Elizabeth Suchi, Demachki Sâmia, Artigiani Ricardo, Assumpção Paulo Pimentel, Lourenço Laércio Gomes, Burbano Rommel Rodríguez, Smith Marília Cardoso

机构信息

Disciplina de Genética, Departamento de Morfologia e Genética, Universidade Federal de São Paulo, Rua Botucatu, 740, São Paulo, 04023900, Brazil.

Núcleo de Pesquisas em Oncologia, Hospital João de Barros Barreto, Universidade Federal do Pará, Avenida Mundurucus, 4487, Belém, 66073000, Brazil.

出版信息

Clin Exp Med. 2017 Feb;17(1):121-129. doi: 10.1007/s10238-015-0400-3. Epub 2015 Nov 14.

Abstract

CDKN1A is a tumor suppressor gene involved in gastric carcinogenesis and is a potential target for histone deacetylase inhibitor-based therapies. Upregulation of CDKN1A is generally observed in several cell lines after histone deacetylase inhibitor treatment; however, little is known about the histone acetylation status associated with this gene in clinical samples, including gastric tumor tissue samples. Therefore, our goal was to quantify the H3K9 and H4K16 acetylation levels associated with three CDKN1A regions in 21 matched pairs of gastric adenocarcinoma and corresponding adjacent non-tumor samples by chromatin immunoprecipitation and to correlate these data with the gene expression. Our results demonstrated that the -402, -20, and +182 CDKN1A regions showed a significantly increased acetylation level in at least one of the histones evaluated (p < 0.05, for all comparisons), and these levels were positively correlated in gastric tumors. However, an inverse correlation was detected between both H3K9 and H4K16 acetylation at the -402 CDKN1A region and mRNA levels in gastric tumors (r = -0.51, p = 0.02; r = -0.60, p < 0.01, respectively). Furthermore, increased H4K16 acetylation at the -20 CDKN1A region was associated with gastric tumors of patients without lymph node metastasis (p = 0.04). These results highlight the complexity of these processes in gastric adenocarcinoma and contribute to a better understanding of CDKN1A regulation in carcinogenesis.

摘要

CDKN1A是一种参与胃癌发生的肿瘤抑制基因,是基于组蛋白去乙酰化酶抑制剂疗法的潜在靶点。组蛋白去乙酰化酶抑制剂处理后,几种细胞系中通常会观察到CDKN1A上调;然而,在包括胃肿瘤组织样本在内的临床样本中,与该基因相关的组蛋白乙酰化状态鲜为人知。因此,我们的目标是通过染色质免疫沉淀法量化21对匹配的胃腺癌及相应癌旁非肿瘤样本中与三个CDKN1A区域相关的H3K9和H4K16乙酰化水平,并将这些数据与基因表达相关联。我们的结果表明,CDKN1A的-402、-20和+182区域在至少一种评估的组蛋白中显示出乙酰化水平显著增加(所有比较中p < 0.05),并且这些水平在胃肿瘤中呈正相关。然而,在胃肿瘤中,-402 CDKN1A区域的H3K9和H4K16乙酰化与mRNA水平之间均检测到负相关(r = -0.51,p = 0.02;r = -0.60,p < 0.01)。此外,-20 CDKN1A区域H4K16乙酰化增加与无淋巴结转移患者的胃肿瘤相关(p = 0.04)。这些结果突出了胃腺癌中这些过程的复杂性,并有助于更好地理解CDKN1A在癌变过程中的调控。

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